Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
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DOID:0070467 | carpal tunnel syndrome 2 | HGNC:2227 | Homo sapiens (human) | 1311 | COMP |
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DOID:0070467 | carpal tunnel syndrome 2 | RGD:2378 | Rattus norvegicus (Norway rat) | 25304 | Comp |
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DOID:0070467 | carpal tunnel syndrome 2 | FB:FBgn0031850 | Drosophila melanogaster (fruit fly) | 33941 | Tsp | CG11326 |
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DOID:0070466 | carpal tunnel syndrome 1 | Xenbase:XB-GENE-865269 | Xenopus laevis (African clawed frog) | 397787 | ttr.L |
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DOID:0070466 | carpal tunnel syndrome 1 | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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DOID:0070466 | carpal tunnel syndrome 1 | MGI:98865 | Mus musculus (house mouse) | 22139 | Ttr |
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DOID:0070466 | carpal tunnel syndrome 1 | RGD:3916 | Rattus norvegicus (Norway rat) | 24856 | Ttr |
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DOID:0070464 | mitochondrial complex V (ATP synthase) deficiency nuclear type 7 | RGD:621379 | Rattus norvegicus (Norway rat) | 192241 | Atp5po |
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DOID:0070463 | mitochondrial complex V (ATP synthase) deficiency nuclear type 5 | RGD:621372 | Rattus norvegicus (Norway rat) | 245965 | Atp5f1d |
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DOID:0070462 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4B | RGD:619993 | Rattus norvegicus (Norway rat) | 65262 | Atp5f1a |
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DOID:0070462 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4B | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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DOID:0070462 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4B | MGI:88115 | Mus musculus (house mouse) | 11946 | Atp5f1a |
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DOID:0070461 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | RGD:619993 | Rattus norvegicus (Norway rat) | 65262 | Atp5f1a |
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DOID:0070461 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | MGI:88115 | Mus musculus (house mouse) | 11946 | Atp5f1a |
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DOID:0070461 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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DOID:0070459 | hereditary spastic paraplegia 90A | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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DOID:0070458 | hereditary spastic paraplegia 89 | WB:WBGene00009164 | Caenorhabditis elegans | 172833 | hrdl-1 |
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DOID:0070456 | hereditary spastic paraplegia 87 | HGNC:23787 | Homo sapiens (human) | 57156 | TMEM63C |
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DOID:0070456 | hereditary spastic paraplegia 87 | SGD:S000004231 | Saccharomyces cerevisiae S288C | 850942 | CSC1 |
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DOID:0070454 | hereditary spastic paraplegia 70 | HGNC:6898 | Homo sapiens (human) | 4141 | MARS1 |
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DOID:0070453 | xanthinuria type II | HGNC:18234 | Homo sapiens (human) | 55034 | MOCOS |
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DOID:0070451 | mitochondrial DNA depletion syndrome 20 | HGNC:6600 | Homo sapiens (human) | 3980 | LIG3 |
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DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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DOID:0070450 | mitochondrial DNA depletion syndrome 19 | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.1.0
Last updated: December 9, 2024